Sunday, May 24, 2009
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37th Common
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Studies of the embryonic development of primitive vertebrates, such as the dogfish shark, clearly show that the excretory system arises from a series of tubules, one pair in every segment of the body between the heart and the tail. This continuous series of tubules constitutes the archinephros, the name implying that the kidney of the ancestral vertebrate had some such form as this. Each tubule opens internally to the body cavity and may, in the remote past, have opened separately to the exterior; but in all living vertebrates the tubules open on each side into a longitudinal duct, the archinephric duct. At the posterior end of the body cavity the two archinephric ducts unite before opening to the exterior. Later in development, Bowman’s capsule arises as a diverticulum of each tubule, subsequently becoming indented by the glomerulus. Eventually, the tubules usually lose their internal openings to the body cavity. The most anterior tubules of the archinephros (pronephros) usually degenerate in the adult.
These ducts and tubules also subserve the reproductive function, and for this reason they are also called the urogenital system. The extent to which the ducts and tubules are shared is greater in the male than in the female. In the male the spermatic tubules of the testis connect with the kidney tubules in the middle region of the archinephros (mesonephros), and in some vertebrates (e.g., the frog) where there is no development of the posterior region (metanephros), the tubules of the mesonephros serve to convey both urine and sperm. In the reptiles, birds, and mammals there is greater separation of function, the mesonephros being exclusively genital and the metanephros being exclusively urinary.
In the female, even in the lower vertebrates, the two systems are confluent only at the posterior end. It has been held that the oviduct is a derivative of the archinephric duct, but the evidence for this is not compelling.
In primitive marine animals the blood is almost identical with seawater in composition; in typical freshwater animals the concentration of the blood is about half that of seawater. Many originally marine animals have evolved the ability to live in fresh water; relatively few animals, after having thus evolved, have returned to the sea, and in none of them has the blood returned to its original “seawater” concentration. The earliest fossil vertebrates are found in marine deposits, but the fossil record shows clearly that the early evolution of fishes took place in fresh water. It is assumed that the blood of early freshwater fishes, like that of other freshwater animals, was osmotically equivalent to half-strength seawater. The sharks and rays returned to the sea during the Carboniferous Period, and no doubt at that time they evolved the device of urea retention. The bony fishes returned to the sea later, in the Mesozoic Era, and solved their problem by swallowing seawater and rejecting excess salt at the gills.
We have discussed in detail the mammalian excretory structure,this is additional material regarding excretion in Birds,reptiles,amhibians and fishes.
Birds and reptiles
The main excretory product of birds and reptiles is uric acid. Since their glomeruli are relatively small, so also is their daily volume of urine. Not highly concentrated by mammalian standards—although it may be turbid with crystals of uric acid—the urine of birds and reptiles is conducted not to a urinary bladder but to the terminal portion of the alimentary canal, the cloaca; from the cloaca it is voided with the feces. Like mammals, and unlike the lower vertebrates, birds and reptiles have skins impermeable to water and thus are well adapted to terrestrial life. The relative inability of the kidney to produce concentrated urine is compensated for in birds that possess salt glands, which remove excess salt from their bodies. These organs are modified tear glands that discharge a concentrated solution of sodium chloride through the nostrils. Salt glands enable marine birds to drink seawater with no ill effects.
Amphibians
Direct evidence for the occurrence of filtration at the glomerulus was first provided by experiments on the amphibian kidney. Although amphibians are formally given the status of terrestrial animals, they are poorly adapted to life on land. They excrete nitrogen in the form of urea and cannot produce urine more concentrated than the blood. Their skins are permeable to water. On land amphibians are liable to lose water very rapidly by evaporation. In fresh water they suffer entry of water by osmosis, which is counteracted by the excretion of a large volume of dilute urine. The urine is stored in a large bladder before being voided, providing a reserve of water the animal can use when it comes on land.
When an amphibian leaves the water, a number of physiological adjustments are made that have the effect of conserving water. The rate of glomerular filtration is reduced by restriction of the blood supply, and this together with an increased release of antidiuretic hormone results in the production of a small volume of urine of the same concentration as the blood. Antidiuretic hormone (ADH, also known as vasopressin, which increases the permeability of the distal and collecting tubules to water) also increases the permeability of the bladder to water and allows the stored urine to be reabsorbed into the body.
Fishes
The homeostasis problem is the same for freshwater fishes as for other freshwater animals. Water enters the body by osmosis and salts leach out. To compensate, the kidney (which has large glomeruli) produces a relatively large amount of dilute urine (about 20 percent of the body weight per day). This serves to remove the water but by itself is insufficient to prevent gradual loss of salts. Extremely diluted salts are taken up from the fresh water and transported directly into the blood by certain specialized cells in the gills. Nitrogenous excretion is no problem: some ammonia is carried away in the large volume of dilute urine, but most of it simply escapes to the external medium by diffusing through the gills.
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